Use of 5-methyl-hept-2-en-4-one as a fragrance and/or flavor

ABSTRACT

A perfumed or edible composition comprising an appropriate carrier and an amount of 5-methyl-hept-2-en-4-one effective to impart its fragrance or flavor to the composition. It imparts a fragrance and flavor reminiscent of hazelnut.

This is a division of application Ser. No. 679,180, filed Dec. 7, 1984,U.S. Pat. No. 4,563,365.

The invention relates to the use of 5-methyl-hept-2-en-4-one as afragrance and/or flavor and to fragrance compositions and/or flavoringcompositions containing this substance.

Within the framework of the investigation under which ketols can beobtained by partial hydrogenation of 1,3-diketones,5-methyl-hept-2-en-4-one has been described as an intermediate in thepreparation of the saturated ketone which was used for determination ofthe ketol structure (J. Am. Chem. Soc. 61, 3303 (1939)).

Tetrahedron Letters 23, 335 (1982) describes a reaction mixture whichconsists of 4 parts of 5-methyl-hept-1-en-4-one and 1 part of5-methyl-hept-2-en-4-one.

No data on the properties of 5-methyl-hept-2-en-4-one are known.

It has been found that 5-methyl-hept-2-en-4-one may be used as afragrance and/or flavor.

Moreover, fragrance compositions and/or flavoring compositionscontaining 5-methyl-hept-2-en-4-one have been found.

5-Methyl-hept-2-en-4-one, to be used according to the invention, is avaluable fragrance and/or flavor which in higher concentration has anutty note, in particular a note reminiscent of hazelnut, in greaterdilution exhibits an enhancer action and, in fragrance compositions,imparts greater naturalness, being usable in amounts of 0.01 to 10% byweight, based on the total composition.

5-Methyl-hept-2-en-4-one to be used according to the invention can beobtained for example by reacting 2-butylmagnesium bromide (prepared, forexample, from 2-bromobutane and magnesium filings) with crotonaldehydein ether solution. 5-Methyl-hept-2-en-4-ol is obtained as anintermediate and is oxidized with a mixture of sodium dichromate andsulphuric acid to give 5-methyl-hept-2-en-4-one. The5-methyl-hept-2-en-4-one is obtained as a mixture of the cis- andtrans-isomers, with the latter predominating. The isomer mixture can beseparated into the cis-isomer and trans-isomer by simple methods ofseparation, such as, for example, fractional distillation by a packedcolumn or slotted tube column or preparative gas chromatography.However, it has been found that the use of the individual isomers offersno advantages over the use of the mixture.

The fragrance to be used according to the invention is employed incombination with other fragrances, known per se (Arctander, Perfume andFlavor Chemicals, Montclair, N.J. (USA), 1969) and etheral oils(Arctander, Perfume and Flavor Materials to Natural Origin., Elisabeth,N.J. (USA), 1960) and leads to perfume bases and fragrance compositionshaving highly expressive notes, which are outstandingly suitable forperfuming finished products in the aerosol, detergent and industrialchemicals sector, but especially for the fine perfumery or cosmeticsector, for example for detergents, hair conditioners, foam baths, bathsalt, dishwasher detergents, washing powders, soaps, antiperspirants,powders, creams, shaving lotion, aftershave lotions, air fresheners,toilet cleaners, room sprays, antiperspirant sprays, deodorant sprays,body sprays, insecticide sprays and sun lotions.

The perfume compositions and perfumed products are prepared in acustomary manner, for example by mixing the components.

Moreover, the 5-methyl-hept-2-en-4-one to be used according to theinvention is a valuable flavor distinguished by a surprisingly low tastethreshold. Thus, in 3% strength sucrose solution the perceptionthreshold is at about 5×10⁻⁶ ppm and the recognition threshold at about30×10⁻⁶ ppm.

At the perception threshold 5-methyl-hept-2-en-4-one produces a tastewhich can be described as "soft, buttery, full sensation in the mouth"while at and above the recognition threshold the description of thetaste is "nutty, hazelnut, soft, buttery, full sensation in the mouth".In addition to its specific characterization in the hazelnut directionin appropriate flavoring compositions, it has, in all non-nut types ofcompositions, a particularly rounding effect, and provides morenaturalness through its buttery soft basic fullness.

The flavoring compositions prepared using 5-methyl-hept-2-en-4-one canbe employed in the entire foodstuff and beverage field, in mouth careand in animal feeds. In particular, they are suitable for icings, fruitpastilles, hard caramels, toffee compositions, chocolate compositions,nougat compositions, fat compositions, margarine, edible oil, cakeflours, biscuit compositions, patisserie, extruded products, dairyproducts, sour milk products, drinks, ices, chewing gum, mouth-careagents, tobacco products, ready-cooked meals, meat and sausage products,soups, sauces, preserved vegetables, spirits, vegetable and microbialproteins and all types of industrially produced animal feeds.

The 5-methyl-hept-2-en-4-one according to the invention is employed inamounts of 5×10⁻⁶ ppm to 100 ppm, preferably 3×10⁻⁵ ppm to 10 ppm, basedon the ready-to-consume foodstuff.

PREPARATION Example 1

2-Butylmagnesium bromide is prepared from 24.32 g of magnesium filingsand 137 g of 2-bromobutane in 100 ml of ether. 56 g of crotonaldehydedissolved in 60 ml of ether are added dropwise to the solution at 0° to10° C. The mixture is then boiled for 2 hours under reflux temperature.Thereafter it is cooled, the batch decomposed with icewater/hydrochloric acid and the product extracted, neutralized anddistilled. 56 g of 5-methyl-hept-2-en-4-ol of boiling point 70° C./18 mbare obtained. To 52 g of this alcohol there is slowly added a mixture of40.34 g of sodium dichromate and 54.1 g of sulphuric acid, while coolingwith ice. After a further hour's reaction at room temperature, the batchis extracted with ether, the organic phase is washed until neutral, thesolvent stripped off and the crude product distilled. Redistillationusing a slotted tube column gives 17.2 g of 5-methyl-hept-2-en-4-one ofboiling point 72° C./20 mb.

USE Example 2

A perfume composition having an orange note is prepared by mixing thefollowing components:

    ______________________________________                                        white orange oil 650                                                          linalyl acetate  325                                                          styrolyl acetate 20                                                           95% strength nootkatone                                                                        5                                                                             1000     parts by weight                                     ______________________________________                                    

On addition of 1 part by weight of 5-methyl-hept-2-en-4-one thecomposition acquires a very natural, mandarin-peel and orange-peel note.

EXAMPLE 3

A flavoring composition A with apple flavor is prepared by mixing thefollowing constituents:

    ______________________________________                                        acetaldehyde   10                                                             n-butyl acetate                                                                              50                                                             trans-hex-2-enal                                                                             30                                                             ethyl acetate  30                                                             hexyl acetate  20                                                             n-butyric acid 10                                                             propylene glycol                                                                             850                                                                           1000      parts by weight                                      ______________________________________                                    

A flavoring composition B is prepared by adding 0.002% of5-methyl-hept-2-en-4-one to A.

A and B are added in a dose of 7.5 ppm to a solution of 5% of sucroseand 0.05% of citric acid in water and subjected to a flavor test.Composition B is unanimously preferred to composition A. The flavor ofcomposition B is described as being fuller, more natural, juicier andmore typical of ripe apples.

EXAMPLE 4

A flavoring composition C with vanilla flavor is prepared by mixing thefollowing constituents:

    ______________________________________                                        vanillin       50                                                             ethylvanillin  10                                                             heliptropin    2                                                              diacetyl       2                                                              propylene glycol                                                                             936                                                                           1000      parts by weight                                      ______________________________________                                    

A flavoring composition D is prepared by adding 0.004% of5-methyl-hept-2-en-4-one to C.

C and D are added in a dose of 37.5 ppm to a solution of 5% of sucrosein water and subjected to a flavor test. Composition D is clearlypreferred to composition C. The flavor of composition D is described asfuller, softer and more natural.

EXAMPLE 5

A flavoring composition E with walnut flavor is prepared by mixing thefollowing constituents:

    ______________________________________                                        vanillin         10                                                           methylcyclopentenolone                                                                         30                                                           resorcinol dimethyl ether                                                                      10                                                           maltol           5                                                            propylene glycol 945                                                                           1000      parts by weight                                    ______________________________________                                    

A flavoring composition F is prepared by adding 0.003% to5-methyl-hept-2-en-4-one to E.

F and E are added in a dose of 75 ppm to a solution of 5% of sucrose inwater and subjected to a flavor test. Composition F is clearly preferredto composition E. The flavor of composition F is described as fuller,softer and more typical of walnut.

EXAMPLE 6

A flavoring composition G with hazelnut flavor is prepared by mixing thefollowing constituents:

    ______________________________________                                        vanillin         30                                                           benzaldehyde     10                                                           furfurol         5                                                            2-ethyl-3,5(3,6)-                                                                              5                                                            dimethylpyraz1ne                                                              2-methyl-3-ethyl-                                                                              5                                                            pyrazine                                                                      resorcinol dimethyl ether                                                                      50                                                           propylene glycol 895                                                                           1000      parts by weight                                    ______________________________________                                    

A flavoring composition H is prepared by adding 0.05% of5-methyl-hept-2-en-4-one to G.

G and H in a dose of 15 ppm are added to a solution of 5% of sucrose inwater and subjected to a flavor test. Composition H is clearly preferredto composition G. The flavor of composition H is described as fuller,more natural and substantially more typical of hazelnut.

EXAMPLE 7

A flavoring composition I with mushroom flavor is prepared by mixing thefollowing constituents:

    ______________________________________                                        oct-1-en-3-ol  40                                                             hexanol        5                                                              propylene glycol                                                                             955                                                                           1000      parts by weight                                      ______________________________________                                    

A flavoring composition J is prepared by adding 0.01% of5-methyl-hept-2-en-4-one to I.

I and J are added in a dose of 7.5 ppm to a solution of 0.5% of sodiumchloride in water and subjected to a flavor test. Composition J isclearly preferred to composition I. The flavor of composition J isdescribed as fuller, substantially more natural and more typical inmushroom character.

It will be appreciated that the instant specification and examples areset forth by way of illustration and not limitation, and that variousmodifications and changes may be made without departing from the spiritand scope of the present invention.

What is claimed is:
 1. A perfumed composition comprising an appropriatecarrier and an amount of 5-methyl-hept-2-en-4-one effective to impartits fragrance to the composition.
 2. A perfumed composition according toclaim 1, wherein the 5-methyl-hept-2-en-4-one is present in about 0.01to 10% by weight.
 3. A composition according to claim 2, wherein thecarrier is a home care or body care composition.
 4. In the modificationof the fragrance of a composition, the improvement which comprisesemploying as the modifying agent an amount effective therefor of5-methyl-hept-2-en-4-one.
 5. A process according to claim 4, wherein thecomposition is a home care or body care composition.